CA3114240C - Imidazopyridine derivatives as alpha4beta7 integrin inhibitors - Google Patents

Imidazopyridine derivatives as alpha4beta7 integrin inhibitors Download PDF

Info

Publication number
CA3114240C
CA3114240C CA3114240A CA3114240A CA3114240C CA 3114240 C CA3114240 C CA 3114240C CA 3114240 A CA3114240 A CA 3114240A CA 3114240 A CA3114240 A CA 3114240A CA 3114240 C CA3114240 C CA 3114240C
Authority
CA
Canada
Prior art keywords
compound
synthesis
inhibitors
independently selected
disease
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
CA3114240A
Other languages
English (en)
French (fr)
Other versions
CA3114240A1 (en
Inventor
Peter A. Blomgren
Taryn CAMPBELL
Jayaraman Chandrasekhar
Christopher T. Clark
Julian A. Codelli
Kevin S. Currie
Jeffrey E. Kropf
Yasamin MOAZAMI
Nicole NAVA
Leena Patel
Stephane Perreault
Jason K. Perry
Kassandra F. Sedillo
Natalie SEEGER
Kirk L. Stevens
Jennifer Anne Treiberg
Suet C. YEUNG
Zhongdong Zhao
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Gilead Sciences Inc
Original Assignee
Gilead Sciences Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Gilead Sciences Inc filed Critical Gilead Sciences Inc
Publication of CA3114240A1 publication Critical patent/CA3114240A1/en
Application granted granted Critical
Publication of CA3114240C publication Critical patent/CA3114240C/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04—Ortho-condensed systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/444—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/47—Quinolines; Isoquinolines
    • A61K31/4709—Non-condensed quinolines and containing further heterocyclic rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/4965—Non-condensed pyrazines
    • A61K31/497—Non-condensed pyrazines containing further heterocyclic rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/5375—1,4-Oxazines, e.g. morpholine
    • A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/02—Immunomodulators
    • A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/54—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame
    • A61K31/541—Non-condensed thiazines containing further heterocyclic rings

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Epidemiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Immunology (AREA)
  • Rheumatology (AREA)
  • Pain & Pain Management (AREA)
  • Transplantation (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
CA3114240A 2018-10-30 2019-10-29 Imidazopyridine derivatives as alpha4beta7 integrin inhibitors Active CA3114240C (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201862752848P 2018-10-30 2018-10-30
US62/752,848 2018-10-30
PCT/US2019/058599 WO2020092394A1 (en) 2018-10-30 2019-10-29 Imidazopyridine derivatives as alpha4beta7 integrin inhibitors

Publications (2)

Publication Number Publication Date
CA3114240A1 CA3114240A1 (en) 2020-05-07
CA3114240C true CA3114240C (en) 2023-09-05

Family

ID=68582500

Family Applications (1)

Application Number Title Priority Date Filing Date
CA3114240A Active CA3114240C (en) 2018-10-30 2019-10-29 Imidazopyridine derivatives as alpha4beta7 integrin inhibitors

Country Status (9)

Country Link
US (2) US11174256B2 (de)
EP (1) EP3873900A1 (de)
JP (2) JP7214882B2 (de)
KR (1) KR102641718B1 (de)
CN (1) CN112969700A (de)
AU (2) AU2019373244B2 (de)
CA (1) CA3114240C (de)
TW (1) TWI717080B (de)
WO (1) WO2020092394A1 (de)

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2927019T3 (es) 2017-03-28 2022-11-02 Gilead Sciences Inc Combinaciones terapéuticas para el tratamiento de enfermedades hepáticas
CA3073656C (en) 2017-09-22 2024-03-05 Jubilant Epipad LLC Heterocyclic compounds as pad inhibitors
CN111225915B (zh) 2017-10-18 2023-03-07 朱比兰特埃皮帕德有限公司 作为pad抑制剂的咪唑并吡啶化合物
EP3707135A1 (de) 2017-11-06 2020-09-16 Jubilant Prodel LLC Pyrimidinderivate als inhibitoren der pd1/pd-l1-aktivierung
BR112020010322A2 (pt) 2017-11-24 2020-11-17 Jubilant Episcribe Llc composto da fórmula i; composto da fórmula ia; composto da fórmula ib; processo de preparação de compostos da fórmula i; composição farmacêutica; método para o tratamento e/ou prevenção de várias doenças; uso dos compostos; método para o tratamento de câncer; e método para o tratamento e/ou prevenção de uma afecção mediada por prmt5 ou um distúrbio proliferativo ou câncer
SG11202008950PA (en) 2018-03-13 2020-10-29 Jubilant Prodel LLC Bicyclic compounds as inhibitors of pd1/pd-l1 interaction/activation
WO2019200202A1 (en) 2018-04-12 2019-10-17 Morphic Therapeutic, Inc. Antagonists of human integrin (alpha4)(beta7)
CA3115820A1 (en) 2018-10-30 2020-05-07 Gilead Sciences, Inc. Compounds for inhibition of .alpha.4.beta.7 integrin
WO2020092375A1 (en) 2018-10-30 2020-05-07 Gilead Sciences, Inc. Quinoline derivatives as alpha4beta7 integrin inhibitors
CA3114240C (en) 2018-10-30 2023-09-05 Gilead Sciences, Inc. Imidazopyridine derivatives as alpha4beta7 integrin inhibitors
CN112969504B (zh) * 2018-10-30 2024-04-09 吉利德科学公司 用于抑制α4β7整合素的化合物
CN113439078B (zh) 2019-02-19 2024-04-23 吉利德科学公司 Fxr激动剂的固体形式
CA3148613A1 (en) 2019-08-14 2021-02-18 Gilead Sciences, Inc. Phenylalanine derived compounds and their use as inhinitors of alpha 4 beta 7 integrin
CA3154269A1 (en) 2019-10-16 2021-04-22 Matthew G. Bursavich Inhibiting human integrin .alpha.4.beta.7
WO2022083649A1 (zh) * 2020-10-20 2022-04-28 杭州领业医药科技有限公司 哒嗪衍生物的晶型

Family Cites Families (232)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2150550A1 (en) 1992-12-01 1994-06-09 Melissa S. Egbertson Fibrinogen receptor antagonists
AU2958195A (en) 1994-06-29 1996-01-25 Texas Biotechnology Corporation Process to inhibit binding of the integrin alpha 4 beta 1 to vcam-1 or fibronectin
US6248713B1 (en) 1995-07-11 2001-06-19 Biogen, Inc. Cell adhesion inhibitors
EP0845987A4 (de) 1995-08-08 2000-05-24 Fibrogen Inc C - proteinaseinhibitoren zur behandlung von störungen, die mit einer kollagenüberproduktion zusammenhängen
ES2271971T3 (es) 1996-07-25 2007-04-16 Biogen Idec Ma Inc. Inhibidores de la adhesion celular.
WO1998042656A1 (en) 1997-03-21 1998-10-01 Cytel Corporation Novel compounds
ES2257808T3 (es) 1997-05-29 2006-08-01 MERCK & CO., INC. (A NEW JERSEY CORP.) Acidos biarilalcanoicos como inhibidores de adhesion celular.
CA2291778A1 (en) 1997-05-29 1998-12-03 Merck & Co., Inc. Heterocyclic amide compounds as cell adhesion inhibitors
AU728435B2 (en) 1997-05-29 2001-01-11 Merck & Co., Inc. Sulfonamides as cell adhesion inhibitors
DE69818049T2 (de) 1997-06-23 2004-07-15 Tanabe Seiyaku Co., Ltd. Inhibitoren der alpha4-beta1 vermittelten zelladhäsion
BR9811573A (pt) 1997-07-31 2000-09-19 Elan Pharm Inc Compostos de benzila que inibem a adesão de leucócitos mediada por vla-4
KR20010022405A (ko) 1997-07-31 2001-03-15 진 엠. 듀발 Ｖｌａ-4에 의해 매개된 백혈구 유착을 억제하는설포닐화된 디펩타이드 화합물
DE69834642T2 (de) 1997-07-31 2007-05-03 Elan Pharmaceuticals, Inc., South San Francisco Verbindungen mit einer 4-amino-phenylalaningruppe, die die vla-4 vermittelte adhäsion von leukozyten inhibieren
WO1999006431A1 (en) 1997-07-31 1999-02-11 Elan Pharmaceuticals, Inc. Substituted phenylalanine type compounds which inhibit leukocyte adhesion mediated by vla-4
WO1999013898A1 (en) 1997-08-15 1999-03-25 Stefan Niewiarowski EC-3, AN INHIBITOR OF α4β1 AND α4β7 INTEGRINS
BR9811988A (pt) 1997-08-22 2000-09-05 Hoffmann La Roche Derivados de n-alcanoilfenilalanina
CA2301377C (en) 1997-08-22 2009-10-06 F. Hoffmann-La Roche Ag N-aroylphenylalanine derivatives
EP0970965A4 (de) 1997-11-13 2002-07-17 Toray Industries Zyklische peptide und medizinische verwendung davon
US6645939B1 (en) 1997-11-24 2003-11-11 Merck & Co., Inc. Substituted β-alanine derivatives as cell adhesion inhibitors
CA2309338A1 (en) 1997-11-24 1999-06-03 Merck & Co., Inc. Cyclic amino acid derivatives as cell adhesion inhibitors
AU751950B2 (en) 1997-11-24 2002-09-05 Merck & Co., Inc. Substituted beta-alanine derivatives as cell adhesion inhibitors
ATE299023T1 (de) 1997-12-17 2005-07-15 Merck & Co Inc Integrinrezeptor antagonisten
MY153569A (en) 1998-01-20 2015-02-27 Mitsubishi Tanabe Pharma Corp Inhibitors of ?4 mediated cell adhesion
AU3748399A (en) 1998-04-16 1999-11-01 Texas Biotechnology Corporation N,n-disubstituted amides that inhibit the binding of integrins to their receptors
CZ298413B6 (cs) 1998-05-28 2007-09-26 Biogen Idec Ma Inc. Beta-Alaninový derivát, farmaceutická kompozice tento derivát obsahující a použití tohoto derivátu pro prípravu léciva
GB9811969D0 (en) 1998-06-03 1998-07-29 Celltech Therapeutics Ltd Chemical compounds
AU8059598A (en) 1998-06-11 1999-12-30 Merck & Co., Inc. Heterocyclic amide compounds as cell adhesion inhibitors
TW591026B (en) 1998-06-23 2004-06-11 Upjohn Co Inhibitors of alpha4beta1 mediated cell adhesion
WO2000002903A1 (en) 1998-07-10 2000-01-20 Cytel Corporation Cs-1 peptidomimetics, compositions and methods of using the same
WO2000005223A2 (en) 1998-07-23 2000-02-03 Astrazeneca Ab Heterocyclic derivatives and their use as integrin inhibitors
KR20010085630A (ko) 1998-08-26 2001-09-07 앤드류 앵뉴 세포 접착 억제를 조절하는 아자-비사이클
EP1140792A1 (de) 1998-12-14 2001-10-10 American Home Products Corporation 3,4-diamino-3-cyclobutene-1,2-dione derivate welche leukocytenadhesion verursacht von vla-4 inhibieren
GB9828074D0 (en) 1998-12-18 1999-02-17 Glaxo Group Ltd Therapeutically useful compounds
US6545003B1 (en) 1999-01-22 2003-04-08 Elan Pharmaceuticals, Inc. Fused ring heteroaryl and heterocyclic compounds which inhibit leukocyte adhesion mediated by VLA-4
DE60021251D1 (de) 1999-01-22 2005-08-18 Elan Pharm Inc Multizyklische verbindungen zur hemmung der durch vla-4 vermittelten leukozytenadhäsion
WO2000043369A1 (en) 1999-01-22 2000-07-27 Elan Pharmaceuticals, Inc. Compounds which inhibit leukocyte adhesion mediated by vla-4
WO2000043413A2 (en) 1999-01-26 2000-07-27 Elan Pharmaceuticals, Inc. Pyroglutamic acid derivatives and related compounds which inhibit leukocyte adhesion mediated by vla-4
SI1154993T1 (en) 1999-02-18 2004-12-31 F. Hoffmann-La Roche Ag Thioamide derivatives
AU3246600A (en) 1999-03-01 2000-09-21 Elan Pharmaceuticals, Inc. Alpha-aminoacetic acid derivatives useful as alpha 4 beta 7 receptor antagonists
US6265572B1 (en) 1999-04-20 2001-07-24 Hoffmann-La Roche Inc. Pyrrolidincarbonylamino cyclic disulfide anti-inflammatory agents
GB9909409D0 (en) 1999-04-24 1999-06-23 Zeneca Ltd Chemical compounds
RU2263109C2 (ru) 1999-05-07 2005-10-27 Тексэс Байотекнолоджи Копэрейшн ПРОИЗВОДНЫЕ КАРБОНОВЫХ КИСЛОТ (ВАРИАНТЫ), ФАРМАЦЕВТИЧЕСКАЯ КОМПОЗИЦИЯ И СПОСОБ СЕЛЕКТИВНОГО ИНГИБИРОВАНИЯ СВЯЗЫВАНИЯ α4β1 ИНТЕГРИНА У МЛЕКОПИТАЮЩЕГО
EP1189612A4 (de) 1999-06-30 2005-02-16 Daiichi Seiyaku Co Vla-4 hemmende verbindungen
JP3795305B2 (ja) 1999-07-19 2006-07-12 田辺製薬株式会社 医薬組成物
CN1376143A (zh) 1999-07-26 2002-10-23 东丽株式会社 羧酸衍生物及以其作为有效成分的粘连分子抑制剂
EP1741428A3 (de) 1999-08-13 2007-05-09 Biogen Idec MA, Inc. Hemmer der Zelladhäsion
WO2001012183A1 (en) 1999-08-16 2001-02-22 Merck & Co., Inc. Heterocycle amides as cell adhesion inhibitors
AU6909300A (en) 1999-08-20 2001-03-19 Merck & Co., Inc. Substituted ureas as cell adhesion inhibitors
CA2385882C (en) 1999-09-24 2009-11-24 Genentech, Inc. Tyrosine derivatives
AU7961200A (en) 1999-10-29 2001-05-14 Kaken Pharmaceutical Co., Ltd. Urea derivative, process for producing the same, and medicine containing the urea derivative
EP1233013B1 (de) 1999-11-18 2007-02-28 Ajinomoto Co., Inc. Phenylalaninderivate
BR0016172A (pt) 1999-12-06 2002-08-20 4-piridinil-n-acil-l-fenilalaninas
SI1237878T1 (sl) 1999-12-06 2007-08-31 Hoffmann La Roche 4-pirimidinil-n-acil-l-fenilanin
ES2415708T3 (es) 1999-12-16 2013-07-26 Biogen Idec Ma Inc. Métodos de tratamiento de la lesión isquémica o hemorrágica del sistema nervioso central mediante el uso de antagonistas anti-integrina alfa4
DE19962936A1 (de) 1999-12-24 2001-06-28 Bayer Ag Neue beta-Aminosäureverbindungen als Integrinantagonisten
JP4784803B2 (ja) 1999-12-28 2011-10-05 味の素株式会社 新規フェニルアラニン誘導体
GB0001348D0 (en) 2000-01-21 2000-03-08 Astrazeneca Uk Ltd Chemical compounds
GB0001346D0 (en) 2000-01-21 2000-03-08 Astrazeneca Uk Ltd Chemical compounds
AU2882801A (en) 2000-01-28 2001-08-07 Kaken Pharmaceutical Co., Ltd. Azepine derivatives
US20040018192A1 (en) 2000-02-03 2004-01-29 Toshiaki Wakabayashi Integrin expression inhibitors
WO2001056994A1 (en) 2000-02-04 2001-08-09 Biogen, Inc. Integrin antagonists
WO2001068586A2 (en) 2000-03-14 2001-09-20 Novartis Ag α4β1 AND α4β7 INTEGRIN INHIBITORS
WO2001070670A1 (fr) 2000-03-23 2001-09-27 Ajinomoto Co., Inc. Nouveau derive de phenylalanine
US6960597B2 (en) 2000-06-30 2005-11-01 Orth-Mcneil Pharmaceutical, Inc. Aza-bridged-bicyclic amino acid derivatives as α4 integrin antagonists
US6794506B2 (en) 2000-07-21 2004-09-21 Elan Pharmaceuticals, Inc. 3-(heteroaryl) alanine derivatives-inhibitors of leukocyte adhesion mediated by VLA-4
PE20020384A1 (es) 2000-07-21 2002-05-28 Schering Corp PEPTIDOS COMO INHIBIDORES DE LA PROTEASA SERINA NS3/NS4a DEL VIRUS DE LA HEPATITIS C
AU2001278986A1 (en) 2000-07-21 2002-02-05 Elan Pharmaceuticals, Inc. 3-amino-2-(4-aminocarbonyloxy)phenyl-propionic acid derivatives as alpha-4- integrin inhibitors
US7335673B2 (en) 2000-08-11 2008-02-26 Kaken Pharmaceutical Co., Ltd. 2,3-Diphenylpropionic acid derivatives or their salts, medicines or cell adhesion inhibitors containing the same, and their usage
SI1288205T1 (sl) 2000-08-18 2011-05-31 Ajinomoto Kk Novi derivati fenilalanina
US20020035104A1 (en) 2000-08-18 2002-03-21 Genentech, Inc. Integrin receptor inhibitors
MY129000A (en) 2000-08-31 2007-03-30 Tanabe Seiyaku Co INHIBITORS OF a4 MEDIATED CELL ADHESION
CA2422135A1 (en) 2000-09-14 2003-03-13 Toray Industries, Inc. Urea derivatives and adhesion molecule inhibitors containing the same as effective ingredients
CA2423007C (en) 2000-09-25 2010-06-01 Toray Industries, Inc. Spiro derivatives and adhesion molecule inhibitors containing the same as effective ingredients
JP4895067B2 (ja) 2000-09-29 2012-03-14 味の素株式会社 新規フェニルアラニン誘導体
CA2430978C (en) 2000-12-28 2012-05-15 Daiichi Pharmaceutical Co., Ltd. Vla-4 inhibitors
ES2200617B1 (es) 2001-01-19 2005-05-01 Almirall Prodesfarma, S.A. Derivados de urea como antagonistas de integrinas alfa 4.
JP4255285B2 (ja) 2001-02-21 2009-04-15 エーザイ・アール・アンド・ディー・マネジメント株式会社 インテグリン発現抑制を介した血管新生抑制剤の効果を検定する方法
DE60218436T2 (de) 2001-02-22 2007-10-31 Celltech R&D Ltd., Slough Phenylalaninenamidderivate mit einer cyclobutengruppe zur verwendung als integrininhibitoren
ATE443736T1 (de) 2001-06-20 2009-10-15 Asahi Chemical Ind Thermoplastharzzusammensetzung
JP2005022976A (ja) 2001-07-18 2005-01-27 Ajinomoto Co Inc カルボン酸誘導体
JP4164871B2 (ja) 2001-07-26 2008-10-15 味の素株式会社 新規フェニルプロピオン酸誘導体
US7557130B2 (en) 2001-07-26 2009-07-07 Ucb Pharma, S.A. Bicyclic heteroaromatic alanines
JP2003048889A (ja) 2001-08-01 2003-02-21 Ajinomoto Co Inc 新規核酸系化合物
WO2003016907A1 (fr) 2001-08-17 2003-02-27 Eisai Co. Ltd. Reactif de dosage pour antigene de la laminine 5 dans un echantillon biologique et procede de dosage
JPWO2003024933A1 (ja) 2001-09-12 2004-12-24 科研製薬株式会社 ２−フェニル−３−ヘテロアリールプロピオン酸誘導体またはその塩、それを用いた医薬
GB0127423D0 (en) 2001-11-15 2002-01-09 Glaxo Group Ltd Process
WO2003053926A1 (fr) 2001-12-13 2003-07-03 Ajinomoto Co.,Inc. Nouveau derive de phenylalanine
WO2003070709A1 (fr) 2002-02-20 2003-08-28 Ajinomoto Co.,Inc. Nouveau derive de phenylalanine
JP4233353B2 (ja) 2002-02-27 2009-03-04 田辺三菱製薬株式会社 医薬組成物
MY140707A (en) 2002-02-28 2010-01-15 Mitsubishi Tanabe Pharma Corp Process for preparing a phenylalanine derivative and intermediates thereof
JP2003277340A (ja) 2002-03-22 2003-10-02 Toray Ind Inc 接着分子阻害剤及び新規アミノ酸誘導体
US20060241132A1 (en) 2002-03-22 2006-10-26 Toray Industries, Inc. A Corporation Of Japan Spiro derivatives and adhesion molecule inhibitors comprising the same as active ingredient
JPWO2003089410A1 (ja) 2002-04-19 2005-08-25 協和醗酵工業株式会社 フェニルアラニン誘導体
CN1649842A (zh) 2002-04-30 2005-08-03 Ucb公司 2,6－喹啉基和2,6－萘基衍生物、用于制备它们的方法和它们作为vla－4抑制剂的用途
TWI281470B (en) 2002-05-24 2007-05-21 Elan Pharm Inc Heterocyclic compounds which inhibit leukocyte adhesion mediated by alpha4 integrins
TW200307671A (en) 2002-05-24 2003-12-16 Elan Pharm Inc Heteroaryl compounds which inhibit leukocyte adhesion mediated by α 4 integrins
GB0216568D0 (en) 2002-07-17 2002-08-28 Celltech R&D Ltd Chemical compounds
GB0216574D0 (en) 2002-07-17 2002-08-28 Celltech R&D Ltd Chemical compounds
GB0216571D0 (en) 2002-07-17 2002-08-28 Celltech R&D Ltd Chemical compounds
WO2004014844A2 (en) 2002-08-09 2004-02-19 Transtech Pharma, Inc. Aryl and heteroaryl compounds and methods to modulate coagulation
GB0218630D0 (en) 2002-08-10 2002-09-18 Tanabe Seiyaku Co Novel compounds
KR101145252B1 (ko) 2003-01-08 2012-05-24 유니버시티 오브 워싱톤 항균제
US7576101B2 (en) 2003-01-24 2009-08-18 Elan Pharmaceuticals, Inc. Composition for and treatment of demyelinating diseases and paralysis by administration of remyelinating agents
CN101386600B (zh) 2003-02-20 2011-07-06 味之素株式会社 具有喹唑二酮骨架的苯丙氨酸衍生物的制造方法及制造中间体
JP2004277338A (ja) 2003-03-14 2004-10-07 Nippon Soda Co Ltd Ｎ−アシルアミノ酸類の製造方法
ES2219177B1 (es) 2003-05-05 2006-02-16 Almirall Prodesfarma, S.A. Derivados de n-(2-feniletil) sulfamida como antagonistas de la integrina alfa4.
CA2525934A1 (en) 2003-05-20 2004-12-02 Genentech, Inc. Thiocarbamate inhibitors of alpha-4 integrins
PE20050232A1 (es) 2003-06-25 2005-04-01 Elan Pharm Inc Metodo y composiciones para tratar la artritis reumatoide
TWI340134B (en) 2003-07-24 2011-04-11 Daiichi Seiyaku Co Cyclohexanecarboxylic acids
US7501538B2 (en) 2003-08-08 2009-03-10 Transtech Pharma, Inc. Aryl and heteroaryl compounds, compositions and methods of use
US20070099938A1 (en) 2003-10-24 2007-05-03 Ono Pharmaceutical Co., Ltd. Antistress drug and medical use thereof
US20050176755A1 (en) 2003-10-31 2005-08-11 Dyatkin Alexey B. Aza-bridged-bicyclic amino acid derivatives as alpha4 integrin antagonists
ES2383525T3 (es) 2003-11-05 2012-06-21 Sarcode Bioscience Inc. Moduladores de la adhesión celular
WO2005046697A1 (ja) 2003-11-14 2005-05-26 Ajinomoto Co., Inc. フェニルアラニン誘導体の徐放性経口投与製剤
CN100563658C (zh) 2003-11-14 2009-12-02 味之素株式会社 苯丙氨酸衍生物的固体分散体或固体分散体医药制剂
WO2005051925A1 (ja) 2003-11-27 2005-06-09 Ajinomoto Co., Inc. フェニルアラニン誘導体の結晶及びその製造方法
GB0329584D0 (en) 2003-12-20 2004-01-28 Tanabe Seiyaku Co Novel compounds
BRPI0418026A (pt) 2003-12-22 2007-04-17 Ajinomoto Kk derivados de fenilalanina ou sais farmaceuticamente aceitáveis destes, composição farmacêutica, antagonista de alfa4 integrina, e, agente terapêutico ou agente preventivo para doenças
MY140489A (en) 2003-12-26 2009-12-31 Eisai R&D Man Co Ltd 1,2-di (cyclic) substituted benzene compounds
US7595318B2 (en) 2004-01-23 2009-09-29 Elan Pharmaceuticals, Inc. Polyethylene glycol conjugates of heterocycloalkyl carboxamido propanoic acids
KR20070004676A (ko) 2004-02-10 2007-01-09 얀센 파마슈티카 엔.브이. 알파４ 인테그린의 길항제로서의 피리다지논
US20050209232A1 (en) 2004-02-10 2005-09-22 Kent Barbay Pyridazinone ureas as antagonists of alpha4 integrins
WO2005087760A1 (en) 2004-03-10 2005-09-22 Merck & Co., Inc. Vla-4 antagonists
JP2007531735A (ja) 2004-04-01 2007-11-08 エラン ファーマシューティカルズ，インコーポレイテッド ステロイド節約剤および該節約剤を使用する方法
JP2007532681A (ja) 2004-04-16 2007-11-15 ジェネンテック・インコーポレーテッド Ｂ細胞の枯渇を増大させる方法
US7618981B2 (en) 2004-05-06 2009-11-17 Cytokinetics, Inc. Imidazopyridinyl-benzamide anti-cancer agents
TW200610754A (en) 2004-06-14 2006-04-01 Daiichi Seiyaku Co Vla-4 inhibitor
MX2007000228A (es) 2004-07-08 2007-03-30 Elan Pharm Inc Antagonistas de vla-4 multivalentes que comprenden porsiones de polietilenglicol.
US7196112B2 (en) 2004-07-16 2007-03-27 Biogen Idec Ma Inc. Cell adhesion inhibitors
EP1781686B1 (de) 2004-08-16 2009-05-06 Merck & Co., Inc. Vla-4-antagonisten
WO2006028393A1 (en) 2004-09-09 2006-03-16 Auckland Uniservices Limited Novel peptides and methods for the treatment of inflammatory disease
WO2006052962A2 (en) 2004-11-10 2006-05-18 Janssen Pharmaceutica, N.V. Bicyclic triazole a4 integrin inhibitors
KR101274879B1 (ko) 2004-12-20 2013-06-14 에자이 알앤드디 매니지먼트 가부시키가이샤 1-시클로프로필메틸-4-[2-(3,3,5,5-테트라메틸시클로헥실)페닐]피페라진의 염 및 결정
WO2006066780A1 (en) 2004-12-22 2006-06-29 F. Hoffmann-La Roche Ag Combinations of valategrast and montelukast for treating asthma
KR101250889B1 (ko) 2004-12-24 2013-04-04 도레이 카부시키가이샤 글리신 유도체 및 그 용도
WO2006081986A1 (en) 2005-02-07 2006-08-10 F.Hoffmann-La Roche Ag Bambuterol and integrin inhibitor combination
WO2006090234A1 (en) 2005-02-22 2006-08-31 Ranbaxy Laboratories Limited Heterocyclic derivatives as cell adhesion inhibitors
WO2006096807A1 (en) 2005-03-08 2006-09-14 Janssen Pharmaceutica N.V. Aza-bridged-bicyclic amino acid derivatives as alpha 4 integrin antagonists
CN101155798A (zh) 2005-04-14 2008-04-02 默克公司 Vla-4拮抗剂
WO2006112738A1 (en) 2005-04-19 2006-10-26 Auckland Uniservices Limited Novel peptides and methods for the treatment of inflammatory disorders
US20090069376A1 (en) 2005-04-21 2009-03-12 Ping Liu VLA-4 Antagonists
NZ563577A (en) 2005-05-20 2011-04-29 Elan Pharm Inc Imidazolone phenylalanine derivatives as VLA-4 antagonists
CA2609255A1 (en) 2005-05-25 2006-11-30 Eisai R&D Management Co., Ltd. Intermediate in production of [2-(3,3,5,5-tetramethylcyclohexyl)phenyl]piperazine compound
US20090163715A1 (en) 2005-05-25 2009-06-25 Eisai R&D Management Co., Ltd. Intermediate in Production of [2-(3,3,5,5-Tetramethylcyclohexyl)phenyl]Piperazine Compound
JP2008542407A (ja) 2005-06-09 2008-11-27 ユセベ ファルマ ソシエテ アノニム ２，６キノリニル誘導体、それらを調製するための方法及び薬剤としてのそれらの使用
EP2402326A1 (de) 2005-06-21 2012-01-04 Ajinomoto Co., Inc. Kristalle aus Hydrochloridsalzen von Phenylalaninderivaten, Herstellungsverfahren und Verwendung dafür
TW200726767A (en) 2005-07-04 2007-07-16 Astrazeneca Ab Chemical compounds 2
EP1961750B1 (de) 2005-12-13 2013-09-18 Daiichi Sankyo Company, Limited Vla-4-hemmendes arzneimittel
EP1978928B1 (de) 2006-01-18 2010-03-31 F. Hoffmann-la Roche AG Pharmazeutische zusammensetzungen, enthaltend valatograst, und verfahren zu deren herstellung
CA2643838A1 (en) 2006-02-27 2007-09-07 Elan Pharmaceuticals, Inc. Pyrimidinyl sulfonamide compounds which inhibit leukocyte adhesion mediated by vla-4
WO2007100763A2 (en) 2006-02-28 2007-09-07 Elan Pharmaceuticals, Inc. Methods of treating inflammatory and autoimmune diseases with alpha-4 inhibitory compounds
EP2103601B1 (de) 2006-11-22 2012-03-14 Ajinomoto Co., Inc. Verfahren zur herstellung von phenylalaninderivaten mit chinazolindiongerüsten, und zwischenprodukte für die herstellung
WO2008064830A1 (en) 2006-11-27 2008-06-05 Ucb Pharma, S.A. Bicyclic and heterobicyclic derivatives, processes for preparing them and their pharmaceutical uses
MX2009009792A (es) 2007-03-12 2009-09-23 Cytopia Res Pty Ltd Compuestos de fenil amino pirimidina y usos de los mismos.
WO2008125210A1 (en) 2007-04-12 2008-10-23 Ucb Pharma, S.A. Quinoline and naphthalene derivatives, processes for their preparation and their use in treatment of inflammatory diseases
WO2008138591A2 (en) 2007-05-14 2008-11-20 Ucb Pharma, S.A. Bicyclic and heterobicyclic derivatives,processes for preparing them and their uses
TWI519508B (zh) 2007-06-12 2016-02-01 Achaogen Inc 抗菌劑
JP2011506322A (ja) 2007-12-07 2011-03-03 エラン ファーマシューティカルズ，インコーポレイテッド 液性腫瘍を治療するための方法および組成物
WO2009124755A1 (en) 2008-04-08 2009-10-15 European Molecular Biology Laboratory (Embl) Compounds with novel medical uses and method of identifying such compounds
CA2724413C (en) 2008-05-15 2016-10-18 Duke University Compositions and methods relating to heat shock transcription factor activating compounds and targets thereof
PT2310509E (pt) 2008-07-21 2015-05-19 Apogenix Gmbh Moléculas de tnfsf em cadeia simples
KR20100101054A (ko) 2009-03-07 2010-09-16 주식회사 메디젠텍 세포핵에서 세포질로의 ｇｓｋ３의 이동을 억제하는 화합물을 함유하는 세포핵에서 세포질로의 ｇｓｋ３ 이동에 의해 발생되는 질환의 치료 또는 예방용 약학적 조성물
WO2010105363A1 (en) 2009-03-16 2010-09-23 Andrei Yudin Cyclic amino acid molecules and methods of preparing the same
GB0905641D0 (en) 2009-04-01 2009-05-13 Serodus As Compounds
BRPI1015259A2 (pt) 2009-04-27 2016-05-03 Elan Pharm Inc antagonistas de piridinona de integrinas alfa-4
EA201290165A1 (ru) 2009-10-21 2012-11-30 Глаксо Груп Лимитед Способ получения производного фенилаланина
WO2011094890A1 (en) 2010-02-02 2011-08-11 Argusina Inc. Phenylalanine derivatives and their use as non-peptide glp-1 receptor modulators
EP2993173A1 (de) 2010-03-29 2016-03-09 Ajinomoto Co., Inc. Kristalle von Salzen von Phenylalaninderivaten
EP2554169B1 (de) 2010-03-29 2019-11-20 EA Pharma Co., Ltd. Pharmazeutisches präparat mit einem phenylalaninderivat
EP2569331A1 (de) 2010-05-10 2013-03-20 Perseid Therapeutics LLC Polypeptid-inhibitoren von vla4
WO2011150499A1 (en) 2010-05-31 2011-12-08 The Governing Council Of The University Of Toronto A method to insert molecular fragments into cyclic molecules
WO2011159781A2 (en) 2010-06-17 2011-12-22 Senomyx, Inc. Bitter taste modulators
AU2011281132B2 (en) 2010-07-20 2014-01-30 Council Of Scientific & Industrial Research Pyridin- 2 - YL sulfanyl acid esters and process for the preparation thereof
CA2997474C (en) 2010-11-16 2020-12-15 Texas Heart Institute Agonists that enhance binding of integrin-expressing cells to integrin receptors
AU2012212323A1 (en) 2011-02-01 2013-09-12 The Board Of Trustees Of The University Of Illinois HDAC inhibitors and therapeutic methods using the same
CA2854658A1 (en) 2011-11-09 2013-05-16 Aestus Therapeutics, Inc. Methods of treating schizophrenia with phenylalanine enamide derivative inhibitors of .alpha.4 integrin possessing a cyclobutene group
RU2014132564A (ru) 2012-01-27 2016-03-20 Ф. Хоффманн-Ля Рош Аг Хитозан, ковалентно связанный с низкомолекулярным антагонистом интегрина, для нацеленной доставки
WO2013110680A1 (en) 2012-01-27 2013-08-01 F. Hoffmann-La Roche Ag Integrin antagonist conjugates for targeted delivery to cells expressing vla-4
US20130303763A1 (en) 2012-03-30 2013-11-14 Michael D. Gershon Methods and compositions for the treatment of necrotizing enterocolitis
WO2013161904A1 (ja) 2012-04-24 2013-10-31 味の素株式会社 スルホンアミド誘導体及びその医薬用途
US9013997B2 (en) 2012-06-01 2015-04-21 Broadcom Corporation System for performing distributed data cut-through
WO2014052605A1 (en) 2012-09-26 2014-04-03 Kflp Biotech, Llc Compounds for the treatment and prevention of retroviral infections
JPWO2014051056A1 (ja) 2012-09-28 2016-08-22 東レ株式会社 グリシン誘導体の結晶及びその医薬用途
US20150045435A1 (en) 2013-08-06 2015-02-12 Indiana University Research And Technology Corporation Compounds and methods for treating diabetes
JP6399874B2 (ja) 2013-09-20 2018-10-03 エーザイ・アール・アンド・ディー・マネジメント株式会社 化合物の抗炎症効果または免疫抑制効果を予測する方法
PT3064491T (pt) 2013-10-29 2020-02-20 Ea Pharma Co Ltd Derivado de sulfonamida e sua utilização medicinal
JP6483148B2 (ja) 2014-03-14 2019-03-13 エアーピオ セラピューティクス インコーポレイテッド ＨＰＴＰ−β阻害剤
WO2015172196A1 (en) 2014-05-13 2015-11-19 Monash University Heterocyclic compounds and use of same
JP2016037468A (ja) 2014-08-07 2016-03-22 味の素株式会社 スルホンアミド誘導体及びその医薬用途
JP2016037467A (ja) 2014-08-07 2016-03-22 味の素株式会社 スルホンアミド誘導体及びその医薬用途
MX2017002985A (es) 2014-09-10 2017-11-17 Epizyme Inc Inhibidores de smyd.
WO2016051828A1 (ja) 2014-09-29 2016-04-07 味の素株式会社 潰瘍性大腸炎の治療用医薬組成物
US10383842B2 (en) 2015-02-13 2019-08-20 Global Biolife Inc. Method and composition for preventing and treating viral infections
JP2018515424A (ja) 2015-03-10 2018-06-14 ザ リージェンツ オブ ザ ユニバーシティ オブ カリフォルニア 抗アルファｖベータ１インテグリン阻害剤及び使用方法
TN2017000538A1 (en) 2015-07-08 2019-04-12 Axerovision Inc Pharmaceutical compositions comprising an integrin alpha4 antagonist for use in treating ocular inflammatory conditions
HUE061437T2 (hu) 2015-10-23 2023-06-28 Navitor Pharm Inc A Sestrin-GATOR2 kölcsönhatás modulátorai és ezek alkalmazásai
CN105483206B (zh) 2016-01-06 2019-09-13 北京汉氏联合生物技术股份有限公司 一种用vcam-1检测msc促内皮细胞增殖能力的方法
JP6809713B2 (ja) 2016-01-20 2021-01-06 国立大学法人 岡山大学 炎症性腸疾患抑制剤
CN106995439B (zh) 2016-01-26 2019-09-20 镇江圣安医药有限公司 氘取代3-(甲磺酰基)-l-苯丙氨酸衍生物及其药物组合物、药物制剂和用途
WO2017132620A1 (en) 2016-01-29 2017-08-03 La Jolla Institute For Allergy And Immunology Methods and compositions using integrin-based therapeutics
WO2017135471A1 (ja) 2016-02-05 2017-08-10 Ｅａファーマ株式会社 α４β７インテグリン阻害剤
US10562898B2 (en) 2016-02-05 2020-02-18 Ea Pharma Co., Ltd. Substituted benzenesulfonamides as inhibitors of alpha-4 beta-7 integrin activity
EP3509590A4 (de) 2016-09-07 2020-12-02 Pliant Therapeutics, Inc. N-acyl-aminosäure-verbindungen und verfahren zur verwendung
CA3038331A1 (en) 2016-09-28 2018-04-05 Blade Therapeutics, Inc. Calpain modulators and therapeutic uses thereof
WO2018085574A2 (en) 2016-11-02 2018-05-11 Washington University Compositions comprising an integrin inhibitor and agents which interact with a chemokine and methods of use thereof
WO2018085552A1 (en) 2016-11-02 2018-05-11 Saint Louis University Integrin antagonists
DK3538525T3 (da) 2016-11-08 2022-08-29 Bristol Myers Squibb Co 3-substituerede propionsyrer som alpha-v-integrinhæmmere
AR110139A1 (es) 2016-11-08 2019-02-27 Bristol Myers Squibb Co COMPUESTOS MONO Y ESPIROCÍCLICOS QUE CONTIENEN CICLOBUTANO Y AZETIDINA COMO INHIBIDORES DE LA INTEGRINA aV
CA3042693A1 (en) 2016-11-08 2018-05-17 Bristol-Myers Squibb Company Pyrrole amides as .alpha.v integrin inhibitors
MX2019005243A (es) 2016-11-08 2019-08-05 Squibb Bristol Myers Co Derivados de indazol como antagonistas de integrina alfa v.
MA46746A (fr) 2016-11-08 2019-09-18 Bristol Myers Squibb Co Amides d'azole et amines en tant qu'inhibiteurs d'intégrine alpha v
RU2769702C2 (ru) 2017-02-28 2022-04-05 Морфик Терапьютик, Инк. Ингибиторы интегрина avb6
MA47692A (fr) 2017-02-28 2020-01-08 Morphic Therapeutic Inc Inhibiteurs de l'intégrine (alpha-v) (bêta-6)
WO2018200625A1 (en) 2017-04-26 2018-11-01 Navitor Pharmaceuticals, Inc. Modulators of sestrin-gator2 interaction and uses thereof
US10246451B2 (en) 2017-04-26 2019-04-02 Aviara Pharmaceuticals, Inc. Propionic acid derivatives and methods of use thereof
US10875875B2 (en) 2017-04-26 2020-12-29 Aviara Pharmaceuticals, Inc. Propionic acid derivatives and methods of use thereof
JP2019031449A (ja) 2017-08-04 2019-02-28 Ｅａファーマ株式会社 スルホンアミド誘導体及びそれを含有する医薬組成物
CN109721605B (zh) 2017-10-31 2022-03-11 维眸生物科技（上海）有限公司 一种免疫细胞迁徙抑制剂
MX2020004455A (es) 2017-11-07 2020-07-24 Bristol Myers Squibb Co Derivados de pirrolopirazina como inhibidores de integrina alfa v.
BR112020018064A2 (pt) 2018-03-07 2020-12-22 Pliant Therapeutics, Inc. Compostos de aminoácidos e métodos de uso
CA3092345A1 (en) 2018-03-13 2019-09-19 The Regents Of The University Of California Inhibitors of integrin alpha 2 beta 1 and methods of use
WO2019200202A1 (en) 2018-04-12 2019-10-17 Morphic Therapeutic, Inc. Antagonists of human integrin (alpha4)(beta7)
WO2020033724A1 (en) 2018-08-08 2020-02-13 The General Hospital Corporation Integrin antagonists
BR112021002839A2 (pt) 2018-08-17 2021-05-11 Oxurion NV antagonistas de integrina
EP3843727A4 (de) 2018-08-29 2022-08-17 Morphic Therapeutic, Inc. Inhibitoren von (alpha-v)(beta-6)-integrin
MX2021002181A (es) 2018-08-29 2021-07-15 Morphic Therapeutic Inc Inhibicion de la integrina alfa v beta 6.
EP3843728A4 (de) 2018-08-29 2022-05-25 Morphic Therapeutic, Inc. Inhibitoren von (alpha-v)(beta-6)-integrin
CA3114240C (en) 2018-10-30 2023-09-05 Gilead Sciences, Inc. Imidazopyridine derivatives as alpha4beta7 integrin inhibitors
WO2020092375A1 (en) 2018-10-30 2020-05-07 Gilead Sciences, Inc. Quinoline derivatives as alpha4beta7 integrin inhibitors
CA3115820A1 (en) 2018-10-30 2020-05-07 Gilead Sciences, Inc. Compounds for inhibition of .alpha.4.beta.7 integrin
CN112969504B (zh) 2018-10-30 2024-04-09 吉利德科学公司 用于抑制α4β7整合素的化合物
CA3148613A1 (en) 2019-08-14 2021-02-18 Gilead Sciences, Inc. Phenylalanine derived compounds and their use as inhinitors of alpha 4 beta 7 integrin

Also Published As

Publication number Publication date
JP7214882B2 (ja) 2023-01-30
US11174256B2 (en) 2021-11-16
AU2019373244B2 (en) 2022-05-26
AU2019373244A1 (en) 2021-04-29
EP3873900A1 (de) 2021-09-08
TWI717080B (zh) 2021-01-21
AU2022218459A1 (en) 2022-09-08
KR20210087480A (ko) 2021-07-12
US20220135561A1 (en) 2022-05-05
US20200165248A1 (en) 2020-05-28
JP2022509512A (ja) 2022-01-20
WO2020092394A1 (en) 2020-05-07
CA3114240A1 (en) 2020-05-07
KR102641718B1 (ko) 2024-02-29
JP2022162077A (ja) 2022-10-21
CN112969700A (zh) 2021-06-15
TW202030190A (zh) 2020-08-16

Similar Documents

Publication Publication Date Title
CA3114240C (en) Imidazopyridine derivatives as alpha4beta7 integrin inhibitors
CA3115830C (en) Compounds for inhibition of .alpha.4.beta.7 integrin
CA3116769C (en) Quinoline derivatives as alpha4beta7 integrin inhibitors
US11224600B2 (en) Compounds for inhibition of alpha 4 beta 7 integrin
AU2020329207B2 (en) Compounds for inhibition of alpha 4 beta 7 integrin

Legal Events

Date Code Title Description
EEER Examination request

Effective date: 20210324

EEER Examination request

Effective date: 20210324

EEER Examination request

Effective date: 20210324

EEER Examination request

Effective date: 20210324

EEER Examination request

Effective date: 20210324

EEER Examination request

Effective date: 20210324

EEER Examination request

Effective date: 20210324

EEER Examination request

Effective date: 20210324